SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
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Browse genes associated with cancer risk that contain miRNA related somatic mutations |
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Somatic mutations that alter miRNA target sites: CLASH [2 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_014897 | ZNF652 | chr17:g.49298658C>T |
NM_014897 | ZNF652 | chr17:g.49298678T>C |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [37 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0044411 | ZNF652 | chr17:g.49293442T>A |
hsa_circ_0044411 | ZNF652 | chr17:g.49304680A>G |
hsa_circ_0044416 | ZNF652 | chr17:g.49317746A>G |
hsa_circ_0044411 | ZNF652 | chr17:g.49298435A>C |
hsa_circ_0044411 | ZNF652 | chr17:g.49298493C>A |
hsa_circ_0044411 | ZNF652 | chr17:g.49298493C>T |
hsa_circ_0044411 | ZNF652 | chr17:g.49298522C>A |
hsa_circ_0044411 | ZNF652 | chr17:g.49298546C>T |
hsa_circ_0044411 | ZNF652 | chr17:g.49298611G>T |
hsa_circ_0044411 | ZNF652 | chr17:g.49298613C>T |
hsa_circ_0044411 | ZNF652 | chr17:g.49298702C>T |
hsa_circ_0044411 | ZNF652 | chr17:g.49298880A>T |
hsa_circ_0044411 | ZNF652 | chr17:g.49298894G>A |
hsa_circ_0044411 | ZNF652 | chr17:g.49298906G>C |
hsa_circ_0044413 | ZNF652 | chr17:g.49311358T>G |
hsa_circ_0044413 | ZNF652 | chr17:g.49311360G>T |
hsa_circ_0044413 | ZNF652 | chr17:g.49311365G>A |
hsa_circ_0044413 | ZNF652 | chr17:g.49311382C>T |
hsa_circ_0044413 | ZNF652 | chr17:g.49311997C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49312727C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49312740A>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49312826C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49316879C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49317242G>A |
hsa_circ_0044416 | ZNF652 | chr17:g.49317266G>A |
hsa_circ_0044416 | ZNF652 | chr17:g.49317273T>C |
hsa_circ_0044416 | ZNF652 | chr17:g.49317430A>G |
hsa_circ_0044416 | ZNF652 | chr17:g.49317432G>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49317440G>C |
hsa_circ_0044416 | ZNF652 | chr17:g.49317458G>A |
hsa_circ_0044416 | ZNF652 | chr17:g.49317463C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49317506G>A |
hsa_circ_0044416 | ZNF652 | chr17:g.49317517C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49317621C>T |
hsa_circ_0044416 | ZNF652 | chr17:g.49317670T>C |
hsa_circ_0044416 | ZNF652 | chr17:g.49317675G>A |
hsa_circ_0044416 | ZNF652 | chr17:g.49317715C>T |
Somatic mutations that alter predicted mRNA-miRNA target sites [36 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001145365 | ZNF652 | chr17:g.49289227A>T |
NM_014897 | ZNF652 | chr17:g.49296697G>T |
NM_014897 | ZNF652 | chr17:g.49289228A>G |
NM_001145365 | ZNF652 | chr17:g.49296679T>A |
NM_001145365 | ZNF652 | chr17:g.49295158G>A |
NM_014897 | ZNF652 | chr17:g.49295158G>A |
NM_001145365 | ZNF652 | chr17:g.49295698G>C |
NM_014897 | ZNF652 | chr17:g.49295698G>C |
NM_001145365 | ZNF652 | chr17:g.49296697G>T |
NM_001145365 | ZNF652 | chr17:g.49289228A>G |
NM_014897 | ZNF652 | chr17:g.49296679T>A |
NM_014897 | ZNF652 | chr17:g.49289227A>T |
NM_014897 | ZNF652 | chr17:g.49289215A>- |
NM_001145365 | ZNF652 | chr17:g.49289215A>- |
NM_014897 | ZNF652 | chr17:g.49290174A>C |
NM_001145365 | ZNF652 | chr17:g.49290174A>C |
NM_014897 | ZNF652 | chr17:g.49291935A>G |
NM_001145365 | ZNF652 | chr17:g.49291935A>G |
NM_014897 | ZNF652 | chr17:g.49297628T>A |
NM_001145365 | ZNF652 | chr17:g.49297628T>A |
NM_014897 | ZNF652 | chr17:g.49293192T>G |
NM_001145365 | ZNF652 | chr17:g.49293192T>G |
NM_014897 | ZNF652 | chr17:g.49296999C>T |
NM_001145365 | ZNF652 | chr17:g.49296999C>T |
NM_014897 | ZNF652 | chr17:g.49293442T>A |
NM_001145365 | ZNF652 | chr17:g.49293442T>A |
NM_014897 | ZNF652 | chr17:g.49294551G>A |
NM_001145365 | ZNF652 | chr17:g.49294551G>A |
NM_014897 | ZNF652 | chr17:g.49293107C>G |
NM_001145365 | ZNF652 | chr17:g.49293107C>G |
NM_014897 | ZNF652 | chr17:g.49297348T>G |
NM_001145365 | ZNF652 | chr17:g.49297348T>G |
NM_014897 | ZNF652 | chr17:g.49295537T>C |
NM_001145365 | ZNF652 | chr17:g.49295537T>C |
NM_014897 | ZNF652 | chr17:g.49296729T>C |
NM_001145365 | ZNF652 | chr17:g.49296729T>C |